Trait
Vestibular hyporeflexia
A general descriptive term that describes impaired functioning of the vestibular apparatus that leads to manifestations such as dizziness or postural imbalance
Summary
- Also called
- Vestibular deficiency, Vestibular dysfunction, Vestibular failure, Vestibular hypofunction, Vestibular loss, Vestibulopathy
- Body system
- Abnormality of the ear
Reference genomeGRCh38hg38
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Get my Genome Test9 genes linked to Vestibular hyporeflexia
Changes in these genes cause rare conditions in which Vestibular hyporeflexia is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| SLC9A1solute carrier family 9 member A1 | Always | In 1 condition |
| ARSGarylsulfatase G | Very often (80–99%) | In 1 condition |
| CEP78centrosomal protein 78 | Very often (80–99%) | In 1 condition |
| CLRN1clarin 1 | Very often (80–99%) | In 1 condition |
| HARS1histidyl-tRNA synthetase 1 | Very often (80–99%) | In 1 condition |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Very often (80–99%) | In 1 condition |
| OTOGotogelin | Often (30–79%) | In 1 condition |
| OTOGLotogelin like | Sometimes (5–29%) | In 1 condition |
| USH1CUSH1 protein network component harmonin | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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